FDAApril 6, 2016device

Bronchoscope Intended to provide optical visualization of and therapeutic access to the Airway and Bronchial Tree. This anatomy includes, but is not restricted to, the organs, tissues and subsystems: Nasal Passage, Trachea and Bronchial Tree. The instrument is introduced via the mouth or the nose...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Pentax has become aware that operational/cleaning accessories and therapeutic devices (e.g., clips, stents, balloons, etc.) can become lodged in an endoscope's instrument channel.

What to do

FDA enforcement status: Terminated

Brands named

pentax medicalpentax

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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